Source | Evidence on protein | Close homologs |
---|---|---|
Cuervo et al. | no | yes: 0 |
Hassani et al. | no | yes: 0 |
Forrest at al. (metacyclic) | no | yes: 0 |
Forrest at al. (procyclic) | no | yes: 3 |
Silverman et al. | no | yes: 0 |
Pissara et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Pires et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Silverman et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
Jamdhade et al. | no | yes: 0 |
Source | Evidence on protein | Close homologs |
---|---|---|
DeepLoc | ||
SignalP6 | no | yes: 0, no: 11 |
NetGPI | no | yes: 0, no: 11 |
Term | Name | Level | Count |
---|---|---|---|
GO:0016020 | membrane | 2 | 12 |
GO:0110165 | cellular anatomical entity | 1 | 12 |
GO:0005783 | endoplasmic reticulum | 5 | 1 |
GO:0005794 | Golgi apparatus | 5 | 1 |
GO:0043226 | organelle | 2 | 1 |
GO:0043227 | membrane-bounded organelle | 3 | 1 |
GO:0043229 | intracellular organelle | 3 | 1 |
GO:0043231 | intracellular membrane-bounded organelle | 4 | 1 |
Related structures:
AlphaFold database: A4H6N2
Term | Name | Level | Count |
---|---|---|---|
GO:0006497 | protein lipidation | 5 | 1 |
GO:0006605 | protein targeting | 5 | 1 |
GO:0006612 | protein targeting to membrane | 5 | 1 |
GO:0006807 | nitrogen compound metabolic process | 2 | 1 |
GO:0006810 | transport | 3 | 1 |
GO:0006886 | intracellular protein transport | 4 | 1 |
GO:0006897 | endocytosis | 5 | 1 |
GO:0008104 | protein localization | 4 | 1 |
GO:0008152 | metabolic process | 1 | 1 |
GO:0009987 | cellular process | 1 | 1 |
GO:0015031 | protein transport | 4 | 1 |
GO:0016192 | vesicle-mediated transport | 4 | 1 |
GO:0018193 | peptidyl-amino acid modification | 5 | 1 |
GO:0018198 | peptidyl-cysteine modification | 6 | 1 |
GO:0018230 | peptidyl-L-cysteine S-palmitoylation | 7 | 1 |
GO:0018231 | peptidyl-S-diacylglycerol-L-cysteine biosynthetic process from peptidyl-cysteine | 7 | 1 |
GO:0018345 | protein palmitoylation | 6 | 1 |
GO:0019538 | protein metabolic process | 3 | 1 |
GO:0033036 | macromolecule localization | 2 | 1 |
GO:0036211 | protein modification process | 4 | 1 |
GO:0043170 | macromolecule metabolic process | 3 | 1 |
GO:0043412 | macromolecule modification | 4 | 1 |
GO:0043543 | protein acylation | 5 | 1 |
GO:0044238 | primary metabolic process | 2 | 1 |
GO:0045184 | establishment of protein localization | 3 | 1 |
GO:0046907 | intracellular transport | 3 | 1 |
GO:0051179 | localization | 1 | 1 |
GO:0051234 | establishment of localization | 2 | 1 |
GO:0051641 | cellular localization | 2 | 1 |
GO:0051649 | establishment of localization in cell | 3 | 1 |
GO:0051668 | localization within membrane | 3 | 1 |
GO:0070727 | cellular macromolecule localization | 3 | 1 |
GO:0071702 | organic substance transport | 4 | 1 |
GO:0071704 | organic substance metabolic process | 2 | 1 |
GO:0071705 | nitrogen compound transport | 4 | 1 |
GO:0072657 | protein localization to membrane | 4 | 1 |
GO:0090150 | establishment of protein localization to membrane | 4 | 1 |
GO:1901564 | organonitrogen compound metabolic process | 3 | 1 |
Term | Name | Level | Count |
---|---|---|---|
GO:0003824 | catalytic activity | 1 | 12 |
GO:0016409 | palmitoyltransferase activity | 5 | 12 |
GO:0016417 | S-acyltransferase activity | 5 | 12 |
GO:0016740 | transferase activity | 2 | 12 |
GO:0016746 | acyltransferase activity | 3 | 12 |
GO:0016747 | acyltransferase activity, transferring groups other than amino-acyl groups | 4 | 12 |
GO:0019706 | protein-cysteine S-palmitoyltransferase activity | 4 | 12 |
GO:0019707 | protein-cysteine S-acyltransferase activity | 3 | 12 |
GO:0140096 | catalytic activity, acting on a protein | 2 | 12 |
Leishmania | From | To | Domain/Motif | Score |
---|---|---|---|---|
CLV_C14_Caspase3-7 | 12 | 16 | PF00656 | 0.635 |
CLV_NRD_NRD_1 | 157 | 159 | PF00675 | 0.499 |
CLV_NRD_NRD_1 | 276 | 278 | PF00675 | 0.398 |
CLV_NRD_NRD_1 | 284 | 286 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 289 | 291 | PF00675 | 0.364 |
CLV_NRD_NRD_1 | 378 | 380 | PF00675 | 0.365 |
CLV_NRD_NRD_1 | 513 | 515 | PF00675 | 0.384 |
CLV_NRD_NRD_1 | 517 | 519 | PF00675 | 0.442 |
CLV_PCSK_FUR_1 | 511 | 515 | PF00082 | 0.407 |
CLV_PCSK_KEX2_1 | 157 | 159 | PF00082 | 0.496 |
CLV_PCSK_KEX2_1 | 284 | 286 | PF00082 | 0.398 |
CLV_PCSK_KEX2_1 | 289 | 291 | PF00082 | 0.365 |
CLV_PCSK_KEX2_1 | 378 | 380 | PF00082 | 0.370 |
CLV_PCSK_KEX2_1 | 496 | 498 | PF00082 | 0.362 |
CLV_PCSK_KEX2_1 | 513 | 515 | PF00082 | 0.519 |
CLV_PCSK_KEX2_1 | 516 | 518 | PF00082 | 0.438 |
CLV_PCSK_PC1ET2_1 | 496 | 498 | PF00082 | 0.362 |
CLV_PCSK_PC1ET2_1 | 515 | 517 | PF00082 | 0.451 |
CLV_PCSK_PC7_1 | 285 | 291 | PF00082 | 0.305 |
CLV_PCSK_PC7_1 | 511 | 517 | PF00082 | 0.425 |
CLV_PCSK_SKI1_1 | 290 | 294 | PF00082 | 0.339 |
DOC_CKS1_1 | 47 | 52 | PF01111 | 0.607 |
DOC_MAPK_gen_1 | 496 | 503 | PF00069 | 0.620 |
DOC_PP1_RVXF_1 | 497 | 504 | PF00149 | 0.583 |
DOC_PP2B_LxvP_1 | 21 | 24 | PF13499 | 0.604 |
DOC_PP4_FxxP_1 | 293 | 296 | PF00568 | 0.552 |
DOC_USP7_MATH_1 | 125 | 129 | PF00917 | 0.627 |
DOC_USP7_MATH_1 | 152 | 156 | PF00917 | 0.620 |
DOC_USP7_MATH_1 | 249 | 253 | PF00917 | 0.632 |
DOC_USP7_MATH_1 | 268 | 272 | PF00917 | 0.630 |
DOC_USP7_MATH_1 | 296 | 300 | PF00917 | 0.580 |
DOC_USP7_MATH_1 | 35 | 39 | PF00917 | 0.653 |
DOC_USP7_MATH_1 | 365 | 369 | PF00917 | 0.490 |
DOC_USP7_MATH_1 | 58 | 62 | PF00917 | 0.636 |
DOC_USP7_MATH_1 | 95 | 99 | PF00917 | 0.662 |
DOC_USP7_UBL2_3 | 389 | 393 | PF12436 | 0.475 |
DOC_WW_Pin1_4 | 137 | 142 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 19 | 24 | PF00397 | 0.719 |
DOC_WW_Pin1_4 | 31 | 36 | PF00397 | 0.708 |
DOC_WW_Pin1_4 | 46 | 51 | PF00397 | 0.630 |
LIG_14-3-3_CanoR_1 | 284 | 288 | PF00244 | 0.624 |
LIG_14-3-3_CanoR_1 | 295 | 301 | PF00244 | 0.579 |
LIG_BIR_III_2 | 218 | 222 | PF00653 | 0.605 |
LIG_BRCT_BRCA1_1 | 128 | 132 | PF00533 | 0.631 |
LIG_BRCT_BRCA1_1 | 316 | 320 | PF00533 | 0.308 |
LIG_eIF4E_1 | 353 | 359 | PF01652 | 0.288 |
LIG_FHA_1 | 133 | 139 | PF00498 | 0.617 |
LIG_FHA_1 | 338 | 344 | PF00498 | 0.279 |
LIG_FHA_1 | 347 | 353 | PF00498 | 0.328 |
LIG_FHA_1 | 368 | 374 | PF00498 | 0.425 |
LIG_FHA_2 | 192 | 198 | PF00498 | 0.628 |
LIG_FHA_2 | 7 | 13 | PF00498 | 0.660 |
LIG_LIR_Gen_1 | 225 | 234 | PF02991 | 0.600 |
LIG_LIR_Gen_1 | 340 | 347 | PF02991 | 0.242 |
LIG_LIR_Gen_1 | 411 | 421 | PF02991 | 0.538 |
LIG_LIR_Gen_1 | 480 | 485 | PF02991 | 0.530 |
LIG_LIR_Gen_1 | 488 | 494 | PF02991 | 0.500 |
LIG_LIR_Nem_3 | 225 | 229 | PF02991 | 0.603 |
LIG_LIR_Nem_3 | 317 | 323 | PF02991 | 0.511 |
LIG_LIR_Nem_3 | 340 | 344 | PF02991 | 0.295 |
LIG_LIR_Nem_3 | 411 | 417 | PF02991 | 0.502 |
LIG_LIR_Nem_3 | 480 | 484 | PF02991 | 0.526 |
LIG_LIR_Nem_3 | 488 | 493 | PF02991 | 0.495 |
LIG_Pex14_1 | 316 | 320 | PF04695 | 0.368 |
LIG_SH2_CRK | 353 | 357 | PF00017 | 0.319 |
LIG_SH2_PTP2 | 323 | 326 | PF00017 | 0.338 |
LIG_SH2_SRC | 226 | 229 | PF00017 | 0.603 |
LIG_SH2_SRC | 490 | 493 | PF00017 | 0.524 |
LIG_SH2_STAT5 | 226 | 229 | PF00017 | 0.603 |
LIG_SH2_STAT5 | 323 | 326 | PF00017 | 0.287 |
LIG_SH2_STAT5 | 327 | 330 | PF00017 | 0.293 |
LIG_SH2_STAT5 | 438 | 441 | PF00017 | 0.382 |
LIG_SH2_STAT5 | 453 | 456 | PF00017 | 0.241 |
LIG_SH2_STAT5 | 481 | 484 | PF00017 | 0.503 |
LIG_SH3_3 | 101 | 107 | PF00018 | 0.639 |
LIG_SH3_3 | 115 | 121 | PF00018 | 0.660 |
LIG_SH3_3 | 167 | 173 | PF00018 | 0.652 |
LIG_SH3_3 | 44 | 50 | PF00018 | 0.667 |
LIG_SH3_3 | 498 | 504 | PF00018 | 0.583 |
LIG_SUMO_SIM_anti_2 | 308 | 313 | PF11976 | 0.295 |
LIG_SUMO_SIM_anti_2 | 355 | 360 | PF11976 | 0.315 |
LIG_SUMO_SIM_par_1 | 134 | 140 | PF11976 | 0.753 |
LIG_SUMO_SIM_par_1 | 355 | 360 | PF11976 | 0.414 |
LIG_TYR_ITSM | 486 | 493 | PF00017 | 0.500 |
LIG_WRC_WIRS_1 | 338 | 343 | PF05994 | 0.239 |
LIG_WRC_WIRS_1 | 358 | 363 | PF05994 | 0.332 |
LIG_WRC_WIRS_1 | 417 | 422 | PF05994 | 0.395 |
MOD_CK1_1 | 128 | 134 | PF00069 | 0.623 |
MOD_CK1_1 | 140 | 146 | PF00069 | 0.642 |
MOD_CK1_1 | 419 | 425 | PF00069 | 0.326 |
MOD_CK1_1 | 505 | 511 | PF00069 | 0.659 |
MOD_CK2_1 | 128 | 134 | PF00069 | 0.733 |
MOD_CK2_1 | 140 | 146 | PF00069 | 0.672 |
MOD_CK2_1 | 6 | 12 | PF00069 | 0.623 |
MOD_CK2_1 | 99 | 105 | PF00069 | 0.643 |
MOD_GlcNHglycan | 101 | 104 | PF01048 | 0.576 |
MOD_GlcNHglycan | 142 | 145 | PF01048 | 0.433 |
MOD_GlcNHglycan | 264 | 267 | PF01048 | 0.430 |
MOD_GlcNHglycan | 421 | 424 | PF01048 | 0.344 |
MOD_GlcNHglycan | 504 | 507 | PF01048 | 0.423 |
MOD_GlcNHglycan | 51 | 54 | PF01048 | 0.398 |
MOD_GlcNHglycan | 60 | 63 | PF01048 | 0.498 |
MOD_GlcNHglycan | 79 | 82 | PF01048 | 0.438 |
MOD_GSK3_1 | 128 | 135 | PF00069 | 0.653 |
MOD_GSK3_1 | 13 | 20 | PF00069 | 0.687 |
MOD_GSK3_1 | 27 | 34 | PF00069 | 0.653 |
MOD_GSK3_1 | 378 | 385 | PF00069 | 0.480 |
MOD_GSK3_1 | 505 | 512 | PF00069 | 0.581 |
MOD_GSK3_1 | 77 | 84 | PF00069 | 0.612 |
MOD_GSK3_1 | 95 | 102 | PF00069 | 0.640 |
MOD_N-GLC_1 | 181 | 186 | PF02516 | 0.424 |
MOD_N-GLC_1 | 71 | 76 | PF02516 | 0.404 |
MOD_N-GLC_2 | 392 | 394 | PF02516 | 0.281 |
MOD_N-GLC_2 | 406 | 408 | PF02516 | 0.327 |
MOD_NEK2_1 | 14 | 19 | PF00069 | 0.635 |
MOD_NEK2_1 | 166 | 171 | PF00069 | 0.652 |
MOD_NEK2_1 | 222 | 227 | PF00069 | 0.678 |
MOD_NEK2_1 | 314 | 319 | PF00069 | 0.317 |
MOD_NEK2_1 | 346 | 351 | PF00069 | 0.290 |
MOD_NEK2_1 | 352 | 357 | PF00069 | 0.352 |
MOD_NEK2_1 | 416 | 421 | PF00069 | 0.368 |
MOD_NEK2_1 | 477 | 482 | PF00069 | 0.369 |
MOD_NEK2_1 | 88 | 93 | PF00069 | 0.708 |
MOD_PIKK_1 | 283 | 289 | PF00454 | 0.584 |
MOD_PIKK_1 | 325 | 331 | PF00454 | 0.322 |
MOD_PKA_1 | 378 | 384 | PF00069 | 0.517 |
MOD_PKA_2 | 210 | 216 | PF00069 | 0.667 |
MOD_PKA_2 | 283 | 289 | PF00069 | 0.637 |
MOD_PKA_2 | 378 | 384 | PF00069 | 0.475 |
MOD_Plk_1 | 14 | 20 | PF00069 | 0.620 |
MOD_Plk_1 | 181 | 187 | PF00069 | 0.660 |
MOD_Plk_2-3 | 6 | 12 | PF00069 | 0.617 |
MOD_Plk_4 | 222 | 228 | PF00069 | 0.616 |
MOD_Plk_4 | 315 | 321 | PF00069 | 0.308 |
MOD_Plk_4 | 346 | 352 | PF00069 | 0.314 |
MOD_Plk_4 | 434 | 440 | PF00069 | 0.331 |
MOD_Plk_4 | 477 | 483 | PF00069 | 0.215 |
MOD_ProDKin_1 | 137 | 143 | PF00069 | 0.707 |
MOD_ProDKin_1 | 19 | 25 | PF00069 | 0.721 |
MOD_ProDKin_1 | 31 | 37 | PF00069 | 0.709 |
MOD_ProDKin_1 | 46 | 52 | PF00069 | 0.628 |
MOD_SUMO_rev_2 | 253 | 263 | PF00179 | 0.632 |
MOD_SUMO_rev_2 | 3 | 9 | PF00179 | 0.660 |
TRG_DiLeu_BaLyEn_6 | 118 | 123 | PF01217 | 0.614 |
TRG_ENDOCYTIC_2 | 226 | 229 | PF00928 | 0.603 |
TRG_ENDOCYTIC_2 | 323 | 326 | PF00928 | 0.368 |
TRG_ENDOCYTIC_2 | 353 | 356 | PF00928 | 0.308 |
TRG_ENDOCYTIC_2 | 414 | 417 | PF00928 | 0.495 |
TRG_ENDOCYTIC_2 | 453 | 456 | PF00928 | 0.221 |
TRG_ENDOCYTIC_2 | 481 | 484 | PF00928 | 0.560 |
TRG_ENDOCYTIC_2 | 490 | 493 | PF00928 | 0.465 |
TRG_ER_diArg_1 | 156 | 158 | PF00400 | 0.691 |
TRG_ER_diArg_1 | 283 | 285 | PF00400 | 0.586 |
TRG_ER_diArg_1 | 288 | 290 | PF00400 | 0.570 |
TRG_ER_diArg_1 | 511 | 514 | PF00400 | 0.627 |
TRG_ER_diArg_1 | 516 | 518 | PF00400 | 0.653 |
TRG_NLS_Bipartite_1 | 496 | 518 | PF00514 | 0.604 |
TRG_NLS_MonoCore_2 | 513 | 518 | PF00514 | 0.640 |
TRG_NLS_MonoExtC_3 | 513 | 518 | PF00514 | 0.600 |
TRG_NLS_MonoExtN_4 | 511 | 518 | PF00514 | 0.600 |
TRG_Pf-PMV_PEXEL_1 | 198 | 202 | PF00026 | 0.422 |
Protein | Taxonomy | Sequence identity | Coverage |
---|---|---|---|
A0A0N1I382 | Leptomonas seymouri | 38% | 100% |
A0A3S7WRS6 | Leishmania donovani | 65% | 100% |
A0A3S7WX91 | Leishmania donovani | 33% | 100% |
A4H6N3 | Leishmania braziliensis | 55% | 100% |
A4HV16 | Leishmania infantum | 65% | 100% |
A4HV17 | Leishmania infantum | 41% | 100% |
E9AH03 | Leishmania infantum | 33% | 100% |
E9ANQ1 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 64% | 83% |
E9ANQ2 | Leishmania mexicana (strain MHOM/GT/2001/U1103) | 49% | 100% |
Q4QGX2 | Leishmania major | 63% | 100% |